The following data is part of a premarket notification filed by Bartels Immunodiagnostic Supplies, Inc. with the FDA for Amer. Histo-id Sys Primary Kit.
Device ID | K842326 |
510k Number | K842326 |
Device Name: | AMER. HISTO-ID SYS PRIMARY KIT |
Classification | Kappa, Antigen, Antiserum, Control |
Applicant | BARTELS IMMUNODIAGNOSTIC SUPPLIES, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | DFH |
CFR Regulation Number | 866.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-06-13 |
Decision Date | 1984-08-02 |